Canonical Allele Identifier: CA480537652
Gene: LINC01465 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.62997091G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.62603311G>C , CM000674.2:g.62603311G>C GRCh38
NC_000012.11:g.62997091G>C , CM000674.1:g.62997091G>C GRCh37
NC_000012.10:g.61283358G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_121682.1:n.124C>G